A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026393



Internal ID19115611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27272597..27296887hg38UCSC Ensembl
Innerchr7:27312216..27336506hg19UCSC Ensembl
Innerchr7:27278741..27303031hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3824291
hg1924291
hg1824291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752935
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026393
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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